Canonical Allele Identifier: CA571475036

Gene: SERAC1

Linked Data

• dbSNP Id: rs1562455273
• gnomAD v2: 6-158571458-C-T
• gnomAD v3: 6-158150426-C-T
• gnomAD v4: 6-158150426-C-T
• MyVariant Identifiers: chr6:g.158571458_158571460delinsTAG (hg19) ; chr6:g.158150426_158150428delinsTAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158150426C>T , CM000668.2:g.158150426C>T	GRCh38
NC_000006.11:g.158571458C>T , CM000668.1:g.158571458C>T	GRCh37
NC_000006.10:g.158491446C>T	NCBI36
NG_032889.1:g.22855G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*99+27G>A	ENSP00000475855.1:n.*99+27G>A
ENST00000642244.1:c.265+27G>A	ENSP00000493554.1:n.265+27G>A
ENST00000642903.1:c.265+27G>A	ENSP00000493559.1:n.265+27G>A
ENST00000643093.1:n.315+27G>A
ENST00000644972.1:c.265+27G>A	ENSP00000496451.1:n.265+27G>A
ENST00000645077.1:c.*99+27G>A	ENSP00000496113.1:n.*99+27G>A
ENST00000645172.1:c.*99+27G>A	ENSP00000495367.1:n.*99+27G>A
ENST00000646190.1:n.1496+27G>A
ENST00000646208.1:c.92-3513G>A	ENSP00000493723.1:n.92-3513G>A
ENST00000646410.1:c.226+27G>A	ENSP00000494205.1:n.226+27G>A
ENST00000646562.1:c.*99+27G>A	ENSP00000496087.1:n.*99+27G>A
ENST00000647468.2:c.265+27G>A MANE Select	ENSP00000496731.1:n.265+27G>A
ENST00000648111.1:c.239+27G>A	ENSP00000497275.1:n.239+27G>A
ENST00000367101.5:c.265+27G>A	ENSP00000356068.1:n.265+27G>A
ENST00000367104.7:c.265+27G>A	ENSP00000356071.3:n.265+27G>A
ENST00000606965.5:c.265+27G>A	ENSP00000475808.1:n.265+27G>A
ENST00000607000.1:c.265+27G>A	ENSP00000475788.1:n.265+27G>A
ENST00000607071.5:c.*99+27G>A	ENSP00000475855.1:n.*99+27G>A
ENST00000607742.5:c.*99+27G>A	ENSP00000475523.1:n.*99+27G>A
NM_032861.3:c.265+27G>A	NP_116250.3:n.265+27G>A
NR_073096.1:n.407+27G>A
XM_006715586.1:c.55+27G>A	XP_006715649.1:n.55+27G>A
XM_011536196.1:c.244+27G>A	XP_011534498.1:n.244+27G>A
XM_011536197.1:c.265+27G>A	XP_011534499.1:n.265+27G>A
XM_011536198.1:c.55+27G>A	XP_011534500.1:n.55+27G>A
XR_942606.1:n.266+27G>A
XM_006715586.3:c.55+27G>A	XP_006715649.1:n.55+27G>A
XM_011536196.3:c.244+27G>A	XP_011534498.1:n.244+27G>A
XM_011536198.3:c.55+27G>A	XP_011534500.1:n.55+27G>A
XM_024446573.1:c.265+27G>A	XP_024302341.1:n.265+27G>A
XR_001743697.2:n.346+27G>A
XR_942606.2:n.397+27G>A
NM_032861.4:c.265+27G>A MANE Select	NP_116250.3:n.265+27G>A
NR_073096.2:n.389+27G>A